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Author Details
Full Name
Sebastian M Armasu
Affiliation
Division of Clinical Trials and Biostatistics, Mayo Clinic
ORCID
Career Start Year
2009
Papers
57
H Index
24
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36790339
Methylation Signature Implicated in Immuno-Suppressive Activities in Tubo-Ovarian High-Grade Serous Carcinoma.
Cancer Epidemiol Biomarkers Prev
2023
34782936
MCM3 is a novel proliferation marker associated with longer survival for patients with tubo-ovarian high-grade serous carcinoma.
Virchows Arch
2022
35816189
Molecular Subclasses of Clear Cell Ovarian Carcinoma and Their Impact on Disease Behavior and Outcomes.
Clin Cancer Res
2022
36160147
Computational tumor stroma reaction evaluation led to novel prognosis-associated fibrosis and molecular signature discoveries in high-grade serous ovarian carcinoma.
Front Med (Lausanne)
2022
36154123
Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors.
Circulation
2022
35102242
Identification of sex-specific genetic associations in response to opioid analgesics in a White, non-Hispanic cohort from Southeast Minnesota.
Pharmacogenomics J
2022
35331649
Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.
Genet Med
2022
34697060
DNA Methylation Profiles of Ovarian Clear Cell Carcinoma.
Cancer Epidemiol Biomarkers Prev
2022
34162658
Identification of a Locus Near <i>ULK1</i> Associated With Progression-Free Survival in Ovarian Cancer.
Cancer Epidemiol Biomarkers Prev
2021
32125938
Evaluation of Germline Genetic Testing Criteria in a Hospital-Based Series of Women With Breast Cancer.
J Clin Oncol
2020
33371009
Expert artificial intelligence-based natural language processing characterises childhood asthma.
BMJ Open Respir Res
2020
30576442
Molecular signatures of X chromosome inactivation and associations with clinical outcomes in epithelial ovarian cancer.
Hum Mol Genet
2019
31279243
Genome-wide DNA methylomic differences between dorsolateral prefrontal and temporal pole cortices of bipolar disorder.
J Psychiatr Res
2019
31420334
Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism.
Blood
2019
29594131
A Genome-Wide Search for Bipolar Disorder Risk Loci Modified by Mitochondrial Genome Variation.
Mol Neuropsychiatry
2018
30062862
Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study.
J Pathol Clin Res
2018
29434467
Genomic Analysis Using Regularized Regression in High-Grade Serous Ovarian Cancer.
Cancer Inform
2018
29036934
Identification of Genetic Interaction with Risk Factors Using a Time-To-Event Model.
Int J Environ Res Public Health
2017
28280090
Pooled Clustering of High-Grade Serous Ovarian Cancer Gene Expression Leads to Novel Consensus Subtypes Associated with Survival and Surgical Outcomes.
Clin Cancer Res
2017
28445597
Taller height as a risk factor for venous thromboembolism: a Mendelian randomization meta-analysis.
J Thromb Haemost
2017
28203683
Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thromb Haemost
2017
27545685
Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease.
Parkinsonism Relat Disord
2016
27732966
HNF1B variants associate with promoter methylation and regulate gene networks activated in prostate and ovarian cancer.
Oncotarget
2016
27449892
Assessing health disparities in children using a modified housing-related socioeconomic status measure: a cross-sectional study.
BMJ Open
2016
27253175
Expression signature distinguishing two tumour transcriptome classes associated with progression-free survival among rare histological types of epithelial ovarian cancer.
Br J Cancer
2016
25991289
Using EHR-Linked Biobank Data to Study Metformin Pharmacogenomics.
Stud Health Technol Inform
2015
26306225
Leveraging an Electronic Health Record-Linked Biorepository to Generate a Metformin Pharmacogenomics Hypothesis.
AMIA Jt Summits Transl Sci Proc
2015
26343387
A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.
Nat Genet
2015
24479488
Integrative genomic analysis identifies epigenetic marks that mediate genetic risk for epithelial ovarian cancer.
BMC Med Genomics
2014
25414722
Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records.
Front Genet
2014
25412286
Lack of replication of the GRIN2A-by-coffee interaction in Parkinson disease.
PLoS Genet
2014
24774302
Methylation of leukocyte DNA and ovarian cancer: relationships with disease status and outcome.
BMC Med Genomics
2014
24853948
Genome-wide investigation of regional blood-based DNA methylation adjusted for complete blood counts implicates BNC2 in ovarian cancer.
Genet Epidemiol
2014
24578302
Alpha-synuclein repeat variants and survival in Parkinson's disease.
Mov Disord
2014
24656894
Does α-synuclein have a dual and opposing effect in preclinical vs. clinical Parkinson's disease?
Parkinsonism Relat Disord
2014
24728075
Tumor hypomethylation at 6p21.3 associates with longer time to recurrence of high-grade serous epithelial ovarian cancer.
Cancer Res
2014
23571109
Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.
Hum Mol Genet
2013
23650146
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genet Epidemiol
2013
23382860
Inherited variants in regulatory T cell genes and outcome of ovarian cancer.
PLoS One
2013
23535731
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Nat Genet
2013
23535730
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
Nat Genet
2013
23535648
Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.
Nat Commun
2013
23535649
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
Nat Commun
2013
23507417
Genetic susceptibility loci, environmental exposures, and Parkinson's disease: a case-control study of gene-environment interactions.
Parkinsonism Relat Disord
2013
22253297
Common variation in Nemo-like kinase is associated with risk of ovarian cancer.
Cancer Epidemiol Biomarkers Prev
2012
22532574
Identification of a novel percent mammographic density locus at 12q24.
Hum Mol Genet
2012
22672568
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
J Thromb Haemost
2012
22561516
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Nat Genet
2012
22658654
Genomic determinants of motor and cognitive outcomes in Parkinson's disease.
Parkinsonism Relat Disord
2012
21463476
Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.
J Thromb Haemost
2011
1 - 50 of 57
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Co-authored papers
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9
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Co-authored papers
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Paul D P Pharoah
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Co-authored papers
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Andrew Berchuck
Duke School of Medicine
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John A Heit
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Linda E Kelemen
Hollings Cancer Center, Medical University of South Carolina
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Peter A Fasching
Otto-Friedrich-University Bamberg
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Susan J Ramus
School of Clinical Medicine, University of NSW Sydney, Lowy Cancer Research Centre
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Boris Winterhoff
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